State

Tennessee product recalls

73,718 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total: 7,859
Critical: 1,324
Severe: 1,973
Most recent: 2026-10-28

Of the 7,859 recalls naming Tennessee we have scored against our rubric, 1,324 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,973 (25%) are Severe.

Which agencies issued them

These figures cover only the 7,859 recalls whose distribution notice names Tennessee specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27801–27825 of 81577

ModerateFDA (Devices)·Z-1510-2021·2021-05-05
Smith & Nephew Recalls Mislabeled CANNU-Flex SILK Interference Screws
Smith & Nephew is recalling CANNU-Flex SILK Interference Screws because some boxes were mislabeled, containing 6mm x 20mm screws instead of the labeled 6mm x 30mm size.
Product
CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Usage: used for interference fixation of bone-tendon-bone of soft tissue grafts in anterior cruciate ligament reconstruction, Part Number: 014208
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1495-2021·2021-05-05
Siemens Artis zee X-Ray System Recalled for Cabling Abrasion
Siemens Medical Solutions is recalling 772 Artis zee ceiling-interventional Fluoroscopic X-Ray Systems due to increased cabling abrasion that may limit functionality and disrupt clinical treatment.
Product
Artis zee ceiling-interventional Fluoroscopic X-Ray System Model Number: 10094137
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1515-2021·2021-05-05
Smiths Medical Recalls Palm Cups Due to Incorrect Shipping Box Labels
Smiths Medical ASD Inc. is recalling 682 Palm Cups because shipping box labels may be incorrect. The devices are intended to mobilize bronchial secretions.
Product
Palm Cups - Product Usage: intended to be used to percuss the chest wall to mobilize the secretions within the bronchial tree.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1511-2021·2021-05-05
Donjoy Ultrasling Pro Arm Sling Recalled for Failed Rivet
DJ Orthopedics is recalling Donjoy Ultrasling Pro arm slings because a rivet at the chafe tab may fail. The recall covers units distributed in the US and several international countries.
Product
DONJOY REF:11-0447-9-ULTRASLING PRO, UNIVERSAL, Rx ONLY, UDI:(01)00190446673552 - Product Usage: intended for medical purposes to immobilize the arm, by means of a fabric band suspended from around the neck.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1507-2021·2021-05-05
Datascope Cardiosave Rescue IABP Recalled for Cybersecurity Vulnerabilities
Datascope Corp. is recalling Cardiosave Rescue IABP units due to cybersecurity vulnerabilities in a TCP/IP software library that may cause loss of communication to hospital systems.
Product
Cardiosave Rescue IABP - Product Usage: used to inflate and deflate intra-aortic balloons. It provides temporary support to the left ventricle via the principle of counterpulsation, Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1489-2021·2021-05-05
Ortho-Clinical VITROS Black Reference Slides Recalled for Mislabeling
Ortho-Clinical Diagnostics is recalling VITROS Black Reference Slides incorrectly labeled as White Reference Slides, which may cause analyzer delays.
Product
VITROS¿ Black Reference Slides CATALOG #: J02316 - Product Usage: The Black Reference Slide is a part/ tool used in the reflectometer correction factor adjustment procedure.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1493-2021·2021-05-05
Cytocell Recalls Chromosome X Alpha-Satellite Probes Due to Cross-Reactivity
Cytocell Ltd. is recalling 89 Chromosome X Alpha-Satellite probes because users may observe additional signals at 9q34, contradicting the insert.
Product
Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte Specific Reagents. Model: MPA3481
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1497-2021·2021-05-05
Siemens Recalls ARTIS X-Ray Systems Due to Software Issue
Siemens is recalling 133 ARTIS X-ray systems due to a potential software issue that may require terminating planned procedures.
Product
Interventional Fluoroscopic X-Ray System ARTIS icono biplane- 11327600 ARTIS icono floor- 11327700 ARTIS pheno- 10849000 ARTIS is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1494-2021·2021-05-05
Coltene Whaledent Recalls TMS LINK PLUS Self-Threading Dental Pins
Coltene Whaledent Inc is recalling TMS LINK PLUS Self-Threading Dental Pins because incorrect pins were packaged and distributed. The recall affects 65 packs of 20 pins.
Product
Dental pins - TMS LINK PLUS Self-Threading Pins - Product Usage: implanted into the teeth or for lab use for dental restoration purposes. The normal procedure requires a hole to be drilled into the tissue of a tooth with an intraoral drill prior to installation. Model…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0340-2021·2021-05-05
Teligent Pharma Recalls Betamethasone Dipropionate Ointment Due to Impurity
Teligent Pharma is recalling Betamethasone Dipropionate Ointment 0.05% due to failed impurity specifications. The product is distributed nationwide in 15-gram tubes.
Product
Betamethasone Dipropionate Ointment USP, 0.05% (Augmented), packaged in 15 grams tubes, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 08310, Distributed by: McKesson Corporation dba Sky Packaging 4971 Southbridge Blvd., Suite 101 Memphis, TN 38141, NDC 63739-996-15
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1492-2021·2021-05-05
Boston Scientific Recalls EXALT Controllers Due to Suboptimal Brightness Settings
Boston Scientific is recalling three EXALT Controllers because they may have been programmed with suboptimal brightness settings, resulting in darker than desired images.
Product
EXALT Controller - Product Usage: intended for use with a Boston Scientific endoscope for endoscopic diagnosis, treatment, and video observation. UPN: M00542430
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1502-2021·2021-05-05
Medela AXS Universal Aspiration Tubing Recalled for Incorrect Expiration Date
Medela is recalling AXS Universal Aspiration Tubing because the label displays an incorrect expiration date of 2023-07-24 instead of 2021-07-24.
Product
Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921 - Product Usage: AXS Universal Aspiration Tubing is used with the Dominant Flex Surgical Suction Pump.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0357-2021·2021-05-05
Genentech Recalls Evrysdi Oral Solution Due to Defective Bottle Adapters
Genentech is recalling 2,627 bottles of Evrysdi (risdiplam) for oral solution because some have incorrect press-in-bottle-adapters that do not fit co-packed syringes.
Product
Evrysdi (risdiplam) for oral solution, 60 mg/80mL (0.75mg/mL), 80 mL total volume after constitution, Rx only, Distributed by: Genentech, Inc. NDC:50242-175-05
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0339-2021·2021-05-05
Teligent Pharma Recalls Betamethasone Dipropionate Ointment Due to Impurity Failures
Teligent Pharma is recalling 79,416 tubes of Betamethasone Dipropionate Ointment USP, 0.05% (Augmented) because the product failed impurity specifications.
Product
Betamethasone Dipropionate Ointment USP, 0.05% (Augmented), packaged in 50 grams tubes, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-019-51
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0338-2021·2021-05-05
Teligent Pharma Recalls Betamethasone Dipropionate Ointment Due to Impurity Failure
Teligent Pharma is recalling Betamethasone Dipropionate Ointment 0.05% because it failed impurity specifications for a known degradation product.
Product
Betamethasone Dipropionate Ointment USP, 0.05% (Augmented), packaged in 15 grams tubes, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 08310, NDC 52565-019-15
Category
Drug
Distribution
Distributed nationwide
SevereUSDA FSIS·017-2021·2021-05-04
Bellisio Recalls Spaghetti with Meat Sauce for Undeclared Soy Allergen
Bellisio Foods is recalling approximately 3,927 pounds of Michelina's Spaghetti with Meat Sauce due to misbranding and an undeclared soy allergen.
Product
Bellisio Foods, Inc. — Bellisio Foods, Inc. Recalls Beef Pasta Products Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·21V309000·2021-05-04
2020 Alfa Romeo Stelvio Braking System Defect Increases Crash Risk
Chrysler is recalling the 2020 Alfa Romeo Stelvio due to a defect in the anti-lock braking system. Hard braking can cause the ABS hydraulic control unit rotor shaft to separate, reducing braking performance and increasing crash risk.
Product
ALFA ROMEO — ALFA ROMEO STELVIO, GIULIA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V315000·2021-05-04
Ducati Recalls Motorcycles Due to Rear Brake System Air Ingress
Ducati is recalling specific 2016-2020 models because air may enter the rear brake system, reducing braking effectiveness and increasing crash risk.
Product
DUCATI — DUCATI SUPERSPORT, MONSTER 1200, XDIAVEL, MONSTER 797
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V313000·2021-05-04
Blue Bird Recalls 2018-2022 All American Buses for Fuel Leak Risk
Blue Bird is recalling 2018-2022 All American buses because a fuel rail leak could cause a fire. Owners should contact dealers for free repairs.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS, ALL AMERICAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V314000·2021-05-04
Arcimoto Motorcycles Recalled for Defective Seat Belt Retractors
Arcimoto is recalling certain 2019-2021 motorcycles because the seat belt retractor spool sleeve may crack, preventing the belt from retracting. This increases the risk of injury. Owners should contact Arcimoto for free replacement.
Product
ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V311000·2021-05-04
Arcimoto Electric Vehicles Recalled: Inverter Software Error Causes Battery Shutdown Risk
Arcimoto is recalling 2019-2021 FUV, 2020 Deliverator, 2020-2021 Roadster, and 2021 Rapid Responder vehicles due to a software error that may cause unexpected battery shutdown, increasing crash risk. Owners should contact Arcimoto or NHTSA for remedy details.
Product
ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER, ROADSTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V312000·2021-05-04
Blue Bird Recalls 2018-2022 All American Buses Due to Fuel Leak Risk
Blue Bird is recalling 2018-2022 All American buses because a fuel rail leak could cause a fire. Owners should contact customer service for updates.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, ALL AMERICAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V310000·2021-05-04
2021 Jeep Cherokee Transmission Oil Cooler Hose May Leak and Cause Fire
Chrysler is recalling certain 2021 Jeep Cherokee vehicles because the transmission oil cooler hose may have been incorrectly cured, allowing transmission fluid to leak and increasing the risk of fire. Dealers will inspect and replace the hose for free.
Product
JEEP — JEEP CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V308000·2021-05-03
2021 Hyundai Santa Fe Fuel Pipe Connection Defect Recall
Hyundai is recalling 2021 Santa Fe vehicles with 2.5-litre Turbo engines due to improperly tightened fuel pipe connections that may leak fuel and increase fire risk. The affected vehicles have already been repaired at dealerships at no cost to owners.
Product
HYUNDAI — HYUNDAI SANTA FE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V307000·2021-05-03
Arcimoto Electric Motorcycles Recalled for Steering Angle Sensor Failure
Arcimoto is recalling multiple 2019-2021 motorcycle models due to faulty steering angle sensors that may cause oversteer and increase crash risk. The company will update firmware and replace the idler arm at no cost.
Product
ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER, ROADSTER
Category
Vehicle
Distribution
Distributed nationwide